发明名称 ARYLANILINE AGONISTS OF beta2-ADRENERGIC RECEPTORS, THEIR USING, PHARMACEUTICAL COMPOSITION BASED ON THEREOF AND METHOD FOR MODULATION OF beta2-ADRENERGIC RECEPTORS
摘要 FIELD: organic chemistry, pharmacy. ^ SUBSTANCE: invention relates to novel compounds of the formula (I): their pharmaceutically acceptable salts or solvates, or stereoisomers possessing properties of agonists of beta2-adrenoreceptors, to pharmaceutical composition based on thereof, using the claimed compounds in manufacturing a medicinal agent, and to a method for modulation of beta2-adrenergic receptors. In the formula (I) each among R1-R5 is chosen independently from group comprising hydrogen atom, (C1-C4)-alkyl and Ra wherein alkyl is substituted optionally with substituted chosen from Rb; or R4 and R5 are combined to form group of the formula: -NRdC(=O)C(Rd)=C(Rd)-; R6, R7 and R8 represent hydrogen atom; R9 represents (C1-C4)-alkyl; R10 represents hydrogen atom or (C1-C4)-alkyl; each among R11, R12 and R13 is chosen independently from group including hydrogen atom, (C1-C4)-alkyl, vinyl, cyclohexyl, phenyl, halogen atom, -CO2Rd, -ORd, -S(O)mRd, -N(NRdRe)Rd or -S(O)2NRdRe, 5-6-membered monocyclic heteroaryl comprising 1 or 2 heteroatoms chosen from nitrogen (N), sulfur (S) atoms, 9-membered bicyclic heteroaryl comprising N as a heteroatom and 5-membered heterocycle comprising N as a heteroatom; or R11 and R12 in common with atoms to which they are bound form 6- or 7-membered heterocyclic ring comprising oxygen (O) atom as a heteroatom and wherein for R11-R13 each phenyl or heteroaryl is substituted optionally with 1 or 2 substitutes chosen independently from Rc, and each heterocyclyl is substituted optionally with 1 or 2 substitutes chosen from Rb and Rc; alkyl is substituted optionally with substitute chosen from Rb, and vinyl is substituted optionally with substitute chosen from Rm; w = 0, 1, 2, 3 or 4. Values Ra, Rb, Rc, Rd, Rm and m are given in the invention claim. ^ EFFECT: improved method for modulation, valuable medicinal properties of compounds and pharmaceutical composition. ^ 22 cl, 225 ex
申请公布号 RU2298545(C2) 申请公布日期 2007.05.10
申请号 RU20040117887 申请日期 2002.11.12
申请人 TEREVANS, INK. 发明人 MORAN EHDMUND DZH.;DZHEJKOBSEN DZHON R.;LIDBETTER MAJKL R.;NODUEHLL MEHTT'JU B.;TREHPP SIN DZH.;EHGGEN DZHEMS;CHERCH TIMOTI DZH.
分类号 C07C215/56;C07D295/22;A61K31/136;A61K31/145;A61K31/16;A61K31/18;A61K31/245;A61K31/33;A61K31/357;A61K31/366;A61K31/4152;A61K31/426;A61K31/4402;A61K31/4453;A61K31/4704;A61K31/4709;A61K31/505;A61K31/5375;A61K31/5377;A61K31/63;A61K31/635;A61K45/00;A61P9/00;A61P11/00;A61P11/06;A61P11/08;A61P15/06;A61P25/00;A61P29/00;A61P43/00;C07C215/60;C07C217/70;C07C217/84;C07C217/86;C07C229/38;C07C229/60;C07C233/43;C07C311/44;C07C317/36;C07C323/36;C07C323/37;C07D213/75;C07D213/76;C07D215/22;C07D215/227;C07D215/26;C07D231/22;C07D239/38;C07D239/42;C07D239/46;C07D239/47;C07D277/20;C07D277/46;C07D277/52;C07D311/80;C07D319/18;C07D321/10;C07D401/12;C07D405/12;C07D409/12;C07D413/10;C07D413/12 主分类号 C07C215/56
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